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effects_of_p450_knockdown_by_rnai

Effects of P450 knockdown by RNAi

The results in the table below should be interpreted with caution in the absence of independent confirmation such as in vitro activity, transgenic expression or CRISPR/Cas9 knockout. RNAi is not equally effective in all arthropod species. The effects on pesticide toxicity also need to be carefully evaluated with attention to toxicity levels in controls, levels of target gene transcript after RNAi, and significance of changes (marginal effects ?). In some cases (e.g. CYP4G RNAi) the effects of RNAi on toxicity may be indirect, e.g. through changes in toxicant penetration through the cuticle. Careful analysis of the cited references is therefore needed before any conclusions can be drawn: Caveat emptor.

P450speciesincreased toxicityother phenotypereferencedoi
CYP2 clan
CYP15A1Schistocerca gregaria decrease in spontaneous and FA-stimulated JH III synthesis, accumulation of MF in the CAMarchal et al., 2011doi.org/10.1016/j.ibmb.2010.12.007
CYP15A1Tribolium castaneum no precocious pupation when injected in 3rd, 4th or 5th larval stagesMinakuchi et al., 2015doi.org/10.1016/j.jinsphys.2015.04.008
CYP15A1 Anthonomus grandis no effect Vasquez et al., 2023doi.org/10.3389/fmolb.2023.1073721
CYP15C1Chilo suppressalis delayed development, increased mortalitySun et al., 2020doi.org/10.1002/PS.5789
CYP15F1Reticulitermes flavipes decrease in presoldier formationTarver et al., 2012doi.org/10.1002/arch.21030
CYP18A1Drosophila melanogaster lethality at pupal stage, also for phm-driven (PG), see paper.Guittard et al.,2011 doi.org/10.1016/j.ydbio.2010.09.023
CYP18A1Aethina tumida defects at adult emergenceWu et al., 2022doi.org/10.1002/ps.7146
CYP18A1Bemisia tabaci MEAM1 lower survival of nymphs Luan et al., 2013doi.org/10.1016/j.ibmb.2013.05.012
CYP18A1Bemisia tabaci MED marginal effects on development, see also other genes in that paperLiu et al., 2020doi.org/10.1016/j.pestbp.2020.104602
CYP18A1Henosepilachna vigintioctopunctata (Coleoptera) disruption of pupation and adult emergence Zhang et al. 2024doi.org/10.1002/arch.22111
CYP18A1Solenopsis invictano effect of flonicamid (in queens)Zhang et al., 2024doi.org/10.1021/acs.jafc.4c08903
CYP303A1Drosophila melanogaster eclosion lethalityWu et al., 2019doi.org/10.1016/j.ibmb.2019.103210
CYP303A1Locusta migratoriamalathion, chlorpyrifos, deltamethrin, carbaryllethal - molting/ecdysis disrupted,lower desication tolerance, modified CHC profileWu et al, 2020doi.org/10.1016/j.pestbp.2020.104637
CYP303A1Apis ceranathiamethoxam, dichlorvos, paraquat, deltamethrin Zhang et al., 2019doi: 10.3389/fgene.2019.01000
CYP303A1Nilaparvata lugens lethal molting defects,reduced ecdysteroid levels and signaling, not reversible by 20E Wu et al., 2024doi.org/10.1016/j.ijbiomac.2024.136234
CYP303A1Nilaparvata lugens increased mortality, molting defects,chitin metabolism genes expression altered Du et al., 2024doi.org/10.1002/ps.8479
CYP305B1 (wrongly called CYP316) ON110138Ectropis oblique (Lepidoptera: Geometridae)deltamethrin, fenpropathrin, chlorpyrifos Peng et al., 2022doi.org/10.3390/genes13071141
CYP305E1 (wrongly called CYP305A1)Aphis gossypii slight decrease in venom protease gene expressionLi et al., 2019doi.org/10.1093/jee/toz021
CYP305H1 (wrongly called CYP305A1)Bemisia tabaci (MEAM1)thiamethoxam Zhou et al., 2024doi.org/10.3390/insects15060399
CYP306A1Schistocerca gregaria decreases 20E titer, no effect on moltingMarchal et al. 2011doi.org/10.1016/j.jinsphys.2011.05.009
CYP306A1Tribolium castaneum reduced ecdysteroid titer and defective development Hentze et al., 2013 doi:10.1371/journal.pone.0055131.g005
CYP306A1Sogatella furcifera decrease in 20E titer, lethality and delayed developmentWan et al., 2014doi.org/10.1016/j.gene.2014.07.023
CYP306A1Laodelphax striatellus decrease in 20E titer, lethality and delayed developmentJia et al., 2015doi.org/10.1111/1744-7917.12147
CYP306A1Apis ceranathiamethoxam, dichlorvos, paraquat, deltamethrin Zhang et al., 2019doi: 10.3389/fgene.2019.01000
CYP306A1Locusta migratoria little molting failure L3 to L4Zhang et al., 2022doi.org/10.1111/1744-7917.12907
CYP306A1Chilo suppressalisincreased toxicity of rice and vetiver grass feedingreduced pupation % and pupal weightLu et al., 2022doi.org/10.1016/j.ijbiomac.2022.11.087
CYP306A1Chilo suppressalis decreased larval survival, longer developmental time, lower 20E titerShazad et al., 2022doi.org/10.3390/insects13080731
CYP306A1Macrobrachium nipponense (Decapoda) reduced 20E titer, reduced molting frequencyPan et al., 2022doi.org/10.1016/j.aqrep.2022.101009
CYP306A1Schistocerca gregaria NO effect on the development and shape of growing oocytes in adult females, or on the shape (length/width ratio) of the deposited eggs. Oviposition and hatching success were NOT negatively affected Schellens et al., 2022doi.org/10.3390/ijms23169232
CYP306A1Bemisia tabaciimidacloprid Liu et al.,2023doi.org/10.1002/ps.7569
CYP306A1Lasioderma serricorne (beetle) lower ecdysteroid titer, impaired development Yan et al., 2023[ 10.1127/entomologia/2023/2033
CYP307A2Tribolium castaneum reduced ecdysteroid titer and defective development Hentze et al., 2013 doi:10.1371/journal.pone.0055131.g005
CYP307A2 (wrongly called CYP307A1)Anopheles gambiae reduced ecdysteroid production by ovariesPondeville et al., 2013doi.org/10.1371/journal.pone.0079861
CYP307 (called 307A1)Sitobion avenaeimidacloprid Zhang et al., 2020doi.org/10.1016/j.cropro.2019.105014
CYP307A2Schistocerca gregaria decreases 20E titer, no effect on molting, but see Sugahara et al., 2017Marchal et al. 2011doi.org/10.1016/j.jinsphys.2011.05.009
CYP307A2Schistocerca gregaria decreases 20E titer, multiple effects including precocious metamorphosis, compare with Marchal et al., 2011 Sugahara et al. 2017doi.org/10.1016/j.ydbio.2017.07.007
CYP307A2Schistocerca gregaria effect on the development and shape of growing oocytes in adult females, and on the shape (length/width ratio) of the deposited eggs. Oviposition and hatching success were negatively affected Schellens et al., 2022doi.org/10.3390/ijms23169232
CYP307A2Locusta migratoria molting delay and molting failure Zhang et al., 2022doi.org/10.1111/1744-7917.12907
CYP307A2(wrongly called CYP307A1)Aethina tumida lethal at metamorphosis, downregulates 20E titerWu et al., 2022doi.org/10.1002/ps.7146
CYP307A2Drosophila melanogaster molting arrest at L1, decreased ecdysteroid titerOno et al., 2012doi.org/10.1016/j.bbrc.2012.04.045
CYP307A2Drosophila melanogaster death at L3 moltSaito et al., 2016doi.org/10.1016/j.jinsphys.2016.09.012
CYP307A2Helicoverpa armigera marginal effect on survival +/- 2-tridecanoneZhang et al., 2016 doi.org/10.1186/s12864-016-3277-y
CYP307A2Locusta migratoria molting delay and failureZhang et al.,2022 doi.org/10.1111/1744-7917.12907.
CYP307A2 (wrongly called 307A1)Spodoptera litura lower ecdysone (?) titer in pupal heads, lower chitin synthase A expressionGong et al., 2022 doi.org/10.1016/j.ecoenv.2022.113425
CYP307A2 (wrongly called 307A1)Lasioderma serricorne (beetle) lower ecdysteroid titer, impaired development Yan et al., 2023[ 10.1127/entomologia/2023/2033
CYP307Portunus trituberculatus (Decapoda) no effect on 20E titer over 4 days p.i.Xie et al., 2016doi.org/10.1016/j.cbpa.2016.06.001
CYP307Macrobrachium nipponense (Decapoda) reduced 20E titer, reduced molting frequencyYuan et al., 2021doi.org/10.1016/j. jsbmb.2021.105976
CYP307B1Tribolium castaneum no effect on larval development Hentze et al., 2013 doi:10.1371/journal.pone.0055131.g005
CYP307B1Lygus hesperus indirect evidence of reduced 20E titer, no adult eclosion, nymphal-like appearance, increased mortalityVan Eckert et al., 2016doi.org/10.1111/imb.12242
CYP307B1Nilaparvata lugens lower 20E titer, developmental arrest, ovarian growth arrestZhou et al., 2020doi.org/10.1016/j.ibmb.2020.103428
CYP307Diaphorina citri reduced 20E titer, lower survivorship Zhang et al., 2023doi.org/10.1016/j.pestbp.2023.105361
CYP307Sogatella furcifera lethality and delayed developmentJia et al., 2013 doi.org/10.1186/1471-2199-14-19
CYP307Laodelphax striatellus lethality and delayed developmentJia et al., 2015 doi.org/10.1111/1744-7917.12087
CYP307Tetranychus urticae decrease in ovipositionWang et al., 2023doi.org/10.3390/ijms241914797
CYP369B3Meteorus pulchricornis (Hymenoptera: Braconidae)phoxim, chlorfenapyr, cypermethrin Xing et al., 2021doi.org/10.3390/insects12070651
CYP392A1Tetranychus cinnabarinuscyflumetofen Feng et al., 2023doi.org/10.1111/1744-7917.13151
CYP392A11Tetranychus urticaeabamectin Xu et al., 2021doi.org/10.1002/ps.6130
CYP392A12Tetranychus urticaeabamectin Xu et al., 2021doi.org/10.1002/ps.6130
CYP392A16Tetranychus urticaeabamectin Papapostolou et al., 2022 doi.org/10.1016/j.ibmb.2021.103709
CYP392A26Tetranychus cinnabarinusfenpropathrin Shi et al., 2016doi.org/10.1111/imb.12251
CYP392A28Tetranychus cinnabarinusfenpropathrin Shi et al., 2016doi.org/10.1111/imb.12251
CYP392D8Tetranychus urticaeabamectin Xu et al., 2021doi.org/10.1002/ps.6130
CYP392D11Tetranychus cinnabariusfenpropathrin Shi et al., 2016doi.org/10.1111/imb.12251
CYP3 clan
CYP6A9, 6A19, 6A20, 6A22Drosophila melanogasterno effect on deltamethrin tox. Duneau et al., 2018doi.org/10.1534/g3.118.200537
CYP6A23Drosophila melanogasterdeltamethrin Duneau et al., 2018doi.org/10.1534/g3.118.200537
CYP6B6Helicoverpa armigera increased mortality Zhang et al., 2013doi.org/10.1017/S0007485313000151
CYP6B6Helicoverpa armigerachlorpyrifos, bifenthrin, cyfluthrin Zhao et al., 2016find
CYP6B7Helicoverpa armigerafenvalerate Tang et al., 2016doi.org/10.1002/ps.3336
CYP6B50Spodoptera lituraxanthotoxin Lu et al., 2019doi.org/10.1016/j.pestbp.2019.06.004
CYP6B53Lymantria dispar larval feeding inhibited, delayed growth lower when dsRNA transgenically expressed in poplar hostSun et al., 2022doi.org/10.1111/aab.12752
CYP6G1Drosophila melanogasterimidacloprid,thiamethoxam, NOT fipronil Shah et al., 2011doi.org/ 10.1002/ps.2218
CYP6G1Drosophila melanogasterDDT Gellatly et al., 2015doi.org/10.1016/j.pestbp.2015.01.001
CYP6G1Drosophila melanogasterDDT Kim et al., 2018doi.org/10.1016/j.pestbp.2018.03.003
CYP6H1Schistocerca gregaria no effect on E/20E ratio in hemolymph, no effect on moltingMarchal et al. 2012doi.org/10.1016/j.jinsphys.2012.03.013
CYP6K1Blattella germanicadeltamethrin Tseng et al., 2024doi.org/10.1093/jee/toae057
CYP6P3v1Anopheles sinensisdeltamethrin Guo et al., 2024doi.org/10.1016/j.actatropica.2024.107413
CYP6P3v2Anopheles sinensisdeltamethrin Guo et al., 2024doi.org/10.1016/j.actatropica.2024.107413
CYP6P9aAnopheles funestusclothianidinlower tox of chlorfenapyrTchouakui et al., 2024 doi.org/10.1016/j.celrep.2024.114566
CYP6P14Culex quinquefasciatuspermethrin Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP6T3Drosophila melanogaster low 20E titer and developmental defects but see Shimell & O’Connor 2022Ou et al., 2011doi.org/10.1371/journal.pbio.1001160
CYP6T3Drosophila melanogaster death at L2/L3 molt or L2 precocious metamorphosis but see Shimell & O’Connor 2022Saito et al., 2016doi.org/10.1016/j.jinsphys.2016.09.012
CYP6AA5Aedes aegypticypermethrin (adults and larvae) Soumalia Issa et al., 2024doi.org/10.1002/arch.70013
CYP6AB12Spodoptera litura b-cypermethrin Lu et al., 2019doi.org/10.1016/j.pestbp.2019.07.010
CYP6AA9Culex pipiens pallensdeltamethrin Lv et al., 2016doi.org/10.1007/s00438-015-1109-4
CYP6AB12Spodoptera lituraλ-cyhalothrin Lu et al., 2020doi.org/10.1016/j.jhazmat.2019.121698
CYP6AB12Spodoptera litura gossypol reduced weight gainZhao et al., 2022doi.org/10.1016/j.pestbp.2022.105284
CYP6AB12Spodoptera lituracyantraniliprole Li et al., 2023doi.org/10.1021/acs.jafc.3c04865
CYP6AB14Spodoptera exiguadeltamethrin, gossypol, deltamethrin + gossypol Hafeez et al., 2019doi:10.3390/ijms20092248
CYP6AB14Spodoptera lituraxanthotoxin, flavone, coumarin toxicity, weigth gain, pupal weightWang et al., 2015doi.org/10.1016/j.jinsphys.2015.02.013
CYP6AB51 (?)QZK27674.1Conogethes punctiferalis (Pyraloidea, Crambidae) chlorantraniliprole, emamectin benzoate, λ-cyhalothrin Yuan et al., 2023doi: 10.3389/fphys.2023.1186804
CYP6AB59Spodoptera lituracyantraniliprole Li et al., 2023doi.org/10.1021/acs.jafc.3c04865
CYP6AB60Spodoptera lituratomatine, xanthotoxin, coumarinonly weigth gainSun et al., 2019doi.org/10.1016/j.pestbp.2018.12.006
CYP6AB111 (wrongly called CYP6B7v1)Lymantria disparemamectin benzoate Xu et al., 2024doi.org/10.1016/j.pestbp.2023.105765
CYP6AB196Grapholita molesta (Tortricidae)emamectin benzoate Liu et al., 2023 doi.org/10.3390/ijms242015435
CYP6AB (unnamed)Scirpophaga incertulas (Crambidae) growth impaired, larval mortalityKola et al.,2016doi.org/10.3389/fphys.2016.00020
CYP6AE4 (called 6K1)Bombyx mori lower survival after Bt injectionYi and Wu 2024doi.org/10.1016/j.ijbiomac.2024.136551
CYP6AE7 (called 9E2)Bombyx mori lower survival after Bt injectionYi and Wu 2024doi.org/10.1016/j.ijbiomac.2024.136551
CYP6AE10Spodoptera exiguaλ-cyhalothrin, quercetin, λ-cyhalothrin+quercetin Hafeez et al., 2020doi.org/10.1016/j.sjbs.2019.05.005
CYP6AE14 (17)Helicoverpa armigeradeltamethrin Tao et al., 2012doi.org/10.1111/j.1365-294X.2012.05548.x
CYP6AE14 (17)Helicoverpa armigera reduced growth on gossypol containing dietMao et al., 2007doi.org/10.1038/nbt1352
CYP6AE14 (17)Helicoverpa armigera reduced growth on cottonMao et al., 2011doi.rog/10.1007/s11248-010-9450-1
CYP6AE14Helicoverpa armigera reduced growth and pupation rateJin et al., 2015doi.org/10.1111/pbi.12355
CYP6AE43Spodoptera lituraβ-cypermethrin, λ-cyhalothrin, fenvalerate Xiao & Lu, 2022doi.org/10.1016/j.ijbiomac.2022.08.014
CYP6AE48Spodoptera lituraβ-cypermethrin, λ-cyhalothrin and fenvalerate Xiao & Lu, 2022doi.org/10.1016/j.ijbiomac.2022.08.014
CYP6AE68Spodoptera lituraindoxacarb Hou et al., 2021doi.org/10.1016/j.pestbp.2021.104946
CYP6AE178Hyphantria cuneacoumarinlower survival on 3 out of 7 tested host plantsLi et al., 2024doi.org/10.1016/j.pestbp.2024.106194
CYP6AN4Spodoptera lituracyantraniliprole Li et al., 2023doi.org/10.1021/acs.jafc.3c04865
CYP6AQ83Solenopsis invictaflonicamid (in queens)Zhang et al., 2024doi.org/10.1021/acs.jafc.4c08903
CYP6AS3 (wrongly called CYP6A13)Apis ceranathiamethoxam Lei et al., 2024doi.org/10.1016/j.pestbp.2024.105890
CYP6AS8Apis mellifera decreased 10-HDA levels in heads (from mandibular glands)Wu et al., 2020doi.org/10.1007/s13592-019-00709-5
CYP6AS160Solenopsis invictafipronil Zhang et al., 2021doi.org/10.1017/S0007485321000651
CYP6AS161 (wrongly called CYP6A14)Solenopsis invicta flonicamid Zhang et al., 2023 doi.org/10.1016/j.pestbp.2023.105651
CYP6AX1v2Nilaparvata lugensb-asarone Xu et al., 2021doi.org/10.1016/j.ijbiomac.2020.12.217
CYP6AY1v2Nilaparvata lugenschlorpyrifos, imidacloprid mix Xu et al., 2020
CYP6AY1Nilaparvata lugensimidacloprid Ding et al., 2013doi.org/10.1016/j.ibmb.2013.08.005
CYP6AY1Nilaparvata lugensimidacloprid Bao et al., 2016doi.org/10.1016/j.pestbp.2015.10.020
CYP6AY1Nilaparvata lugensimidacloprid Zhang et al., 2016doi.org/10.1016/j.ibmb.2016.10.009
CYP6BB4Culex pipens pallensdeltamethrin Zou et al., 2019doi.org/10.1111/imb.12571
CYP6BD12Nilaparvata lugensdecreases tox of chlorpyrifos Zhang et al., 2023doi.org/10.1021/acs.jafc.2c08957
CYP6BE1 (wrongly called CYP6K1)Apis ceranaabamectin, imidacloprid Tan et al., 2023doi.org/10.1016/j.pestbp.2023.105377
CYP6BG1Plutella xylostellapermethrin Bautista et al., 2009
CYP6BG1Plutella xylostellachlorantraniliprole, b-cypermethrin ? Li et al., 2018
CYP6BH5Phaedon cochleriae (mustard lef beetle) reduced chrysomelidial level in defenseive secretionFu et al., 2019 doi.org/10.1016/j.ibmb.2019.103212
CYP6BJ1v1Leptinotarsa decemlineataimidacloprid, potato leaf extract Kalsi et al., 2017doi.org/10.1016/j.ibmb.2017.02.002
CYP6BQ7Tribolium castaneumartemisia essential oil Zhang et al., 2021
CYP6BQ8Tribolium castaneumterpinen-4-ol Gao et al., 2023doi.org/10.1017/S0007485322000566
CYP6BQ9Leptinotarsa decemlineatadeltamethrin Zhu et al., 2010
CYP6BQ11Tribolium castaneumdichlorvos, (marginal effect on carbofuran) Xiong et al., 2020doi.org/10.1002/ps.5384
CYP6BY3Culex quinquefasciatusno effect on permethrin toxicity Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP6BZ2Culex quinquefasciatuspermethrin Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP6CM1Bemisia tabacinicotine, imidaclopridhigh toxicity of dsRNA Li et al., 2015doi.org/10.1002/ps.3903
CYP6CR2Dendroctonus armanditerpenoids Liu et al.,2022doi.org/10.1016/j.pestbp.2022.105180
CYP6CS1Nilaparvata lugenspymetrozine Wang et al., 2021doi.org/10.1002/ps.6438
CYP6CS1Nilaparvata lugensno effect onchlorpyrifos tox Zhang et al., 2023doi.org/10.1021/acs.jafc.2c08957
CYP6CS3Sogatella furciferachlorpyrifos Ruan et al., 2021doi.org/10.3390/biology10080795
CYP6CV1 (?)QZK27660.1Conogethes punctiferalis (Pyraloidea, Crambidae) chlorantraniliprole, emamection benzoate, λ-cyhalothrin Yuan et al., 2023doi: 10.3389/fphys.2023.1186804
CYP6CV5Chilo suppressalischlorantraniliprole Xu et al, 2018doi.org/10.1002/ps.5171
CYP6CW1Laodelphax striatellusbuprofezin, pymetrozine Zhang et al., 2017
CYP6CW1Nilaparvata lugensimidacloprid Zhang et al., 2016doi.org/10.1016/j.ibmb.2016.10.009
CYP6CW3v2Laodelphax striatellusethiprole Elsaki et al., 2015
CYP6CX2Bemisia tabacithiamethoxam Yang et al., 2023 JEEdoi.org/10.1093/jee/toad089
CYP6CX3Bemisia tabacicyantraniliprole Zhang et al., 2022doi.org/10.1021/acs.jafc.2c04699
CYP6CX3Bemisia tabacithiamethoxam Yang et al., 2023 JEEdoi.org/10.1093/jee/toad089
CYP6CX4Bemisia tabaciflupyradifurone, imidacloprid Wang et al., 2020
CYP6CX4Bemisia tabaciflupyradifurone Wang et al., 2024doii.org/10.1016/j.ijbiomac.2024.131056
CYP6CY3Aphis gossypiiimidacloprid Wei et al., 2021doi.org/10.1016/j.pestbp.2021.104878
CYP6CY5Aphis gossypiicyantraniliprole Ding et al., 2023doi.org/10.1016/j.ijbiomac.2023.126824
CYP6CY7Aphis gossypiispirotetramat Peng et al.,2022doi.org/10.1002/ps.6818
CYP6CY7Aphis glycinesimidacloprid Li et al., 2024doi.org/10.3390/insects15030188
CYP6CY9Aphis gossypiithiamethoxam, imidacloprid Lv et al., 2022doi.org/10.1021/acs.jafc.2c04867
CYP6CY9Aphis gossypiicyantraniliprole Ding et al., 2023doi.org/10.1016/j.ijbiomac.2023.126824
CYP6CY13Aphis gossypiisulfoxaflor Ma et al., 2019doi.org/10.1016/j.pestbp.2019.03.021
CYP6CY14Aphis gossypiidinotefuran Chen et al., 2020doi.org/10.1016/j.pestbp.2020.104601
CYP6CY14Aphis gossypiiacetamiprid Ullah et al. 2020doi.org/10.1016/j.pestbp.2020.104687
CYP6CY14Aphis gossypiiclothianidin Ullah et al. 2023doi.org/ 10.1127/entomologia/2023/2002
CYP6CY19Aphis gossypiisulfoxaflor Ma et al., 2019doi.org/10.1016/j.pestbp.2019.03.021
CYP6CY19Aphis gossypii increases mortality and reduces fecundity in cotton and cucumber-specialized aphidsGao et al., 2022doi.org/10.1021/acs.jafc.2c05403
CYP6CY21Aphis gossypiispirotetramat Peng et al.,2022doi.org/10.1002/ps.6818
CYP6CY22Aphis gossypiidinotefuran Chen et al., 2020doi.org/10.1016/j.pestbp.2020.104601
CYP6CY22Aphis gossypiithiamethoxam, imidacloprid Lv et al., 2022doi.org/10.1021/acs.jafc.2c04867
CYP6CY22Aphis gossypiicyantraniliprole Ding et al., 2024doi.org/10.1021/acs.jafc.3c08770
CYP6CZ1Aphis gossypiiacetamiprid Ullah et al. 2020doi.org/10.1016/j.pestbp.2020.104687
CYP6CZ1Aphis gossypiithiamethoxam, imidacloprid Lv et al., 2022doi.org/10.1021/acs.jafc.2c04867
CYP6DA1Aphis gossypiicyantraniliprole Ding et al., 2023doi.org/10.1016/j.ijbiomac.2023.126824
CYP6DA2 (wrongly called CYP6A2)Aphis gossypiia- cypermethrin, spirotetramat Peng et al., 2016doi.org/10.1016/j.pestbp.2015.07.008
CYP6DB1Aphis gossypiithiamethoxam, imidacloprid Lv et al., 2022doi.org/10.1021/acs.jafc.2c04867
CYP6DB3Bemisia tabaci Qimidacloprid, thiamethoxam Wei et al., 2023doi.org/10.1016/j.pestbp.2023.105468
CYP6DC1Aphis gossypiiacetamiprid Ullah et al. 2023doi.org/ 10.1127/entomologia/2023/2002
CYP6DC1Rhopalosiphum padiλ-cyhalothrin Wang et al., 2022doi.org/10.1016/j.pestbp.2022.105088
CYP6DE5Dendroctonus armanditerpenoids Liu et al.,2022doi.org/10.1016/j.pestbp.2022.105180
CYP6DF1Dendroctonus armandi(+)-a-pinene Liu & Chen,2022doi.org/10.1016/j.pestbp.2022.105270
CYP6DJ2Dendroctonus armandi(+)-a-pinene Liu & Chen,2022doi.org/10.1016/j.pestbp.2022.105270
CYP6DW3Bemisia tabaciafidopyropen Ma et al.2024doi.org/10.1016/j.jia.2024.07.027
CYP6DW4Bemisia tabacidimpropyridaz Tang et al.2024doi.org/10.1016/j.pestbp.2024.105888
CYP6EM1Bemisia tabacidinetofuran Huang et al.2024doi.org/10.1021/acs.jafc.3c06953
CYP6ER1Nilaparvata lugens Pang et al., 2016
CYP6ER1Nilaparvata lugensimidacloprid Bao et al., 2016doi.org/10.1016/j.pestbp.2015.10.020
CYP6ER1Nilaparvata lugenssulfoxaflor Liao et al., 2018find
CYP6ER1Nilaparvata lugensnitenpyram Mao et al., 2019
CYP6ER1Nilaparvata lugensimidacloprid, thiamethoxam, dinotefuran Sun et al., 2018doi.org/10.1016/j.pestbp.2018.06.014
CYP6ER1Nilaparvata lugensimidacloprid Zhang et al., 2016doi.org/10.1016/j.ibmb.2016.10.009
CYP6ER1Nilaparvata lugensimidacloprid Yokoi et al., 2016doi.org/10.1002/ps.6200
CYP6ER1Nilaparvata lugensimidacloprid Cheng et al., 2021doi.org/10.1016/j.chemosphere.2020.128269
CYP6ER1Nilaparvata lugensnitenpyram, imidacloprid Zhang et al., 2024doi.org/10.1016/j.jare.2024.11.006
CYP6ER1vANilaparvata lugensimidacloprid,nitenpyram,cycloxaprid Gong et al., 2023doi.org/10.1021/acs.jafc.3c03167
CYP6ER4Sogatella furciferachlorpyrifos Ruan et al., 2021doi.org/10.3390/biology10080795
CYP6EX3Chironomus tentanschlorpyriphos toxicity DECREASED Tang et al., 2017doi.org/10.1016/j.chemosphere.2017.07.137
CYP6FD1?Sogatella furciferasulfoxaflor Wang et al., 2019doi.org/10.3390/ijms20184573
CYP6FD1Locusta migratoriadeltamethrin, NOT imidacloprid Liu et al., 2023doi.org/10.1016/j.pestbp.2023.105627
CYP6FD2Locusta migratoriacarbaryl Guo et al., 2016
CYP6FD3Locusta migratoriaNOT deltamethrin, NOT imidacloprid Liu et al., 2023doi.org/10.1016/j.pestbp.2023.105627
CYP6FE1Locusta migratoriaimidacloprid, NOT deltamethrin Liu et al., 2023doi.org/10.1016/j.pestbp.2023.105627
CYP6FE1Locusta migratoriacarbaryl Guo et al., 2016
CYP6FF1Locusta migratoriadeltamethrin Guo et al., 2016
CYP6FJ3 (wrongly called SF01)Sogatella furciferatriflumezopyrim Gong et al., 2022doi.org/10.1016/j.ecoenv.2022.113575
CYP6FJ3Sogatella furciferapymetrozine Gong et al., 2023doi.org/10.1021/acs.jafc.3c03617
CYP6FV12Bradysia odoriphagaimidacloprid Chen et al., 2019doi.org/10.1016/j.pestbp.2018.11.009
CYP6FV21Bradysia odoriphagaimidacloprid,λ-cyhalothrin Zhang et al., 2024 doi.org/10.1021/acs.jafc.3c08807
CYP6HC1Locusta migratoriafluvalinate Zhang et al., 2019doi.org/10.1016/j.chemosphere.2019.02.011
CYP6HL1Locusta migratoriacarbaryl, fluvalinate, cypermethrin Zhang et al., 2019doi.org/10.1016/j.chemosphere.2019.02.011
CYP6HL1Locusta migratoriaNOT deltamethrin, NOT imidacloprid Liu et al., 2023doi.org/10.1016/j.pestbp.2023.105627
CYP6HN1Locusta migratoriacarbaryl, fluvalinate, fenvalerate Zhang et al., 2019doi.org/10.1016/j.chemosphere.2019.02.011
CYP6HQ1Locusta migratoriacarbaryl, fluvalinate Zhang et al., 2019doi.org/10.1016/j.chemosphere.2019.02.011
CYP6MS1Sitophilus zeamaisterpinen-4-ol Huang et al., 2020doi.org/10.1016/j.pestbp.2019.07.008
CYP6MS1Sitophilus zeamaisterpinen-4-ol, limonene Zhao et al., 2023doi.org/10.1016/j.pestbp.2023.105426
CYP6MS5Sitophilus zeamaisterpinen-4-ol, limonene Zhao et al., 2023doi.org/10.1016/j.pestbp.2023.105426
CYP6MS6Sitophilus zeamaisterpinen-4-ol, limonene Zhao et al., 2023doi.org/10.1016/j.pestbp.2023.105426
CYP6MS8Sitophilus zeamaisterpinen-4-ol, limonene Zhao et al., 2023doi.org/10.1016/j.pestbp.2023.105426
CYP6MS9Sitophilus zeamaisterpinen-4-ol, limonene Zhao et al., 2023doi.org/10.1016/j.pestbp.2023.105426
CYP6MU1Locusta migratoriaNOT deltamethrin, NOT imidacloprid Liu et al., 2023doi.org/10.1016/j.pestbp.2023.105627
CYP6MU1Locusta migratoria decrease in antennal EAG response to trans-2-hexen-1-al, nonanal Wu et al., 2023doi.org/10.1016/j.pestbp.2023.105620
CYP6QE1Bradysia odoriphagaimidacloprid,λ-cyhalothrin Zhang et al., 2024 doi.org/10.1021/acs.jafc.3c08807
CYP6SD3Lasioderma serricorne ethyl formate, benzothiazole Li et al., 2024doi.org/10.3389/fphys.2024.1503953
CYP6SN3Chilo suppressalisincreased toxicity of rice and vetiver grass feedingreduced pupation % and pupal weightLu et al., 2022doi.org/10.1016/j.ijbiomac.2022.11.087
CYP6SX1Bradysia odoriphagaclothianidin Zhang et al.,2022 doi.org/10.1021/acs.jafc.2c01315
CYP6SX1Bradysia odoriphagaimidacloprid, phoxim Wang et al.,2022doi.org/10.1021/acs.jafc.4c00358
CYP6ABE1Glyphodes pyloalis (Lepidoptera: Pyralidae)tolfenpyrad Pan et al., 2023 PBP
CYP6AEL1Lasioderma serricorne ethyl formate, benzothiazole Li et al., 2024doi.org/10.3389/fphys.2024.1503953
CYP9A3Locusta migratoriadeltamethrin, permethrin Zhu et al., 2016doi.org/10.1016/j.pestbp.2016.01.001
CYP9A9Spodoptera exigualufenuron, methoxyfenozide Zhang et al.,2023doi.org/10.1111/imb.12829
CYP9A10Spodoptera exigua alpha-cypermethrin, xanthotoxin + alpha-cypermethrin Hafeez et al., 2020doi.org/10.1016/j.pestbp.2019.07.003
CYP9A14Helicoverpa armigeradeltamethrin Tao et al., 2012doi.org/10.1111/j.1365-294X.2012.05548.x
CYP9A21v3Spodoptera exiguachlorantraniliprole Wang et al., 2018
CYP9A40Spodoptera lituraquercetin, cinnamic acid, deltamethrin, methoxyfenozide Wang et al., 2015
CYP9A54 (wrongly called CYP9A23v1)Lymantria disparemamectin benzoate Xu et al., 2024doi.org/10.1016/j.pestbp.2023.105765
CYP9A58Spodoptera frugiperda prolonged developmental timeHe et al. 2023doi.org/10.1002/ps.7355
CYP9A68Chilo suppressalischlorantraniliprole Xu et al, 2018doi.org/10.1002/ps.5171
CYP9A75Spodoptera frugiperdatetraniliprole,emamectin benzoate Wang et al., 2024doi.org/10.1017/S000748532300038X
CYP9A98Spodoptera exiguadeltamethrin, deltamethrin + gossypol Hafeez et al., 2019doi:10.3390/ijms20092248
CYP9A105Spodoptera exiguaa-cypermethrin, deltamethrin, fenvalerate Wang et al., 2018doi.org/10.3390/ijms19030737
CYP9A120Cydia pomonellaλ-cyhalothrin Li et al., 2022doi.org/10.1101/2022.07.22.501203
CYP9A121Cydia pomonellaλ-cyhalothrin Li et al., 2022doi.org/10.1101/2022.07.22.501203
CYP9A157 (wrongly called CYP9A75a)Spodoptera lituracyantraniliprole, a-cypermethrin Li et al., 2024doi.org/10.1021/acs.jafc.4c03069
CYP9A158 (wrongly called CYP9A75b)Spodoptera lituracyantraniliprole, a-cypermethrin Li et al., 2024doi.org/10.1021/acs.jafc.4c04465
CYP9A209Grapholita molesta (Tortricidae)emamectin benzoate Liu et al., 2023 doi.org/10.3390/ijms242015435
CYP9D5 (wrongly called CYP9E2)Tribolium castaneum effects on intermediary metabolism Zhou et al., 2023 doi.org/10.3390/agronomy13092263
CYP9J10Anopheles sinensisdeltamethrin Guo et al., 2024doi.org/10.1016/j.actatropica.2024.107413
CYP9J32Aedes aegyptipermethrin (larvae) Soumalia Issa et al., 2024doi.org/10.1002/arch.70013
CYP9J35Culex pipiens pallensdeltamethrin Guo et al., 2017doi.org/10.1016/j.ibmb.2017.03.006
CYP9J35Culex quinquefasciatuspermethrin Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP9J45Culex quinquefasciatuspermethrin Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP9J57Bradysia odoriphagaclothianidin Zhang et al.,2022 doi.org/10.1021/acs.jafc.2c01315
CYP9K1Anopheles sinensisdeltamethrin Guo et al., 2024doi.org/10.1016/j.actatropica.2024.107413
CYP9M12Culex quinquefasciatusmalathion Huang et al., 2023
CYP9Q1Apis mellifera decreases sugar water consumption, sugar sensitivity (proboscis extension assay), tyrosine hydroxylase and IRS expression in the brain Xu et al., 2024doi.org/10.3390/ijms252413550
CYP9Z5 (wrongly called CYP9F2)Tribolium castaneumlower resistance to CO2 stressaffects carbohydrate metabolism Wang et al., 2024doi.org/10.3390/insects15070502
CYP9Z6Tribolium castaneumterpinen-4-ol Gao et al., 2022doi.org/10.1016/j.pestbp.2022.105065
CYP9Z25Leptinotarsa decemlineataimidacloprid, potato leaf extract Kalsi et al., 2017doi.org/10.1016/j.ibmb.2017.02.002
CYP9Z26Leptinotarsa decemlineataimidacloprid Clements et al., 2017doi.org/10.1016/j.pestbp.2016.07.001
CYP9Z29Leptinotarsa decemlineataimidacloprid, potato leaf extract Kalsi et al., 2017doi.org/10.1016/j.ibmb.2017.02.002
CYP9Z140Leptinotarsa decemlineatathiamethoxam Wang et al., 2024doi.org/10.3390/insects15080559
CYP9AL1Culex quinquefasciatuspermethrin Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP9AQ1Locusta migratoriafluvalinate Zhu et al., 2016doi.org/10.1016/j.pestbp.2016.01.001
CYP9AQ2Locusta migratoriadeltamethrin Guo et al., 2015doi.org/10.1016/j.pestbp.2015.01.003
CYP9AY1Leptinotarsa decemlineatathiamethoxam Wang et al., 2024doi.org/10.3390/insects15080559
CYP41G2Pardosa pseudoannulata no phenotype reportedHou et al.2021doi.org/10.1111/imb.12731
CYP321A7Spodoptera frugiperdaλ-cyhalothrin Li et al. 2024doi.org/10.1016/j.pestbp.2024.106009
CYP321A7Spodoptera lituraλ-cyhalothrinlower larval weight gain:flavone, xanthotoxin, curcuminXiao et al. 2024doi.org/10.1021/acs.jafc.3c05423
CYP321A8Spodoptera frugiperdachlorantraniliprole Bai-Zhong et al. 2020doi.org/10.1093/jisesa/ieaa047
CYP321A8Spodoptera frugiperdachlorpyrifos, deltamethrin Chen et al. 2024doi.org/10.1111/1744-7917.13376
CYP321A8Spodoptera lituraλ-cyhalothrinlower larval weight gain:flavone, xanthotoxin, curcuminXiao et al. 2024doi.org/10.1021/acs.jafc.3c05423
CYP321A9Spodoptera frugiperdachlorantraniliprole Bai-Zhong et al. 2020doi.org/10.1093/jisesa/ieaa047
CYP321A9Spodoptera frugiperdaemamectin benzoate Shi et al. 2023doi.org/10.1093/jee/toad168
CYP321A9Spodoptera frugiperdaferulic acid,gramine,tricineprolonged developmental timeHe et al. 2023doi.org/10.1002/ps.7355
CYP321A10Spodoptera lituraλ-cyhalothrinlower larval weight gain:flavone, xanthotoxinXiao et al. 2024doi.org/10.1021/acs.jafc.3c05423
CYP321A12Spodoptera lituraNOT λ-cyhalothrin Xiao et al. 2024doi.org/10.1021/acs.jafc.3c05423
CYP321A15Spodoptera lituraNOT λ-cyhalothrinlower larval weight gain:flavone, xanthotoxinXiao et al. 2024doi.org/10.1021/acs.jafc.3c05423
CYP321A19Spodoptera litura indoxacarb Li et al., 2023doi.org/10.1016/j.jhazmat.2023.132605
CYP321B1Spodoptera frugiperdachlorantraniliprole Bai-Zhong et al. 2020doi.org/10.1093/jisesa/ieaa047
CYP321B1Spodoptera frugiperdaλ-cyhalothrin Guo et al.,2024doi.org/10.1016/j.pestbp.2024.105916
CYP321B1Spodoptera liturachlopyrifos, β-cypermethrin, NOT methomyl Wang et al., 2017doi.org/10.1111/1744-7917.12315
CYP321B1 (wrongly called CYP6)Spodoptera lituracypermethrin, λ-cyhalothrin, NOT fenvalerate Xu et al., 2020doi.org/10.1016/j.pestbp.2020.104649
CYP321B1Spodoptera litura tannin (decreased weight gain)Zhao et al., 2022doi.org/10.1016/j.ijbiomac.2021.11.144
CYP321E1Plutella xylostellachlorantraniliprole Xu et al, 2018doi.org/10.1002/ps.5171
CYP321F3Chilo suppressalischlorantraniliprole Xu et al, 2018doi.org/10.1002/ps.5171
CYP324A12Chilo suppressalischlorantraniliprole Xu et al, 2018doi.org/10.1002/ps.5171
CYP324A16Spodoptera lituracoumarin Xia et al., 2023 doi.org/10.3390/ijms241713177
CYP336A65 (wrongly called CYP9E2)Solenopsis invicta flonicamid Zhang et al., 2023 doi.org/10.1016/j.pestbp.2023.105651
CYP336A66Solenopsis invictano effect of flonicamid (in queens)Zhang et al., 2024doi.org/10.1021/acs.jafc.4c08903
CYP332A1Spodoptera lituracyantraniliprole Li et al., 2023doi.org/10.1021/acs.jafc.3c04865
CYP337B5Spodoptera frugiperdaλ-cyhalothrin Guo et al.,2024doi.org/10.1016/j.pestbp.2024.105916
CYP337B5Spodoptera frugiperdachlorantraniliprole Guo et al.,2024doi.org/10.1016/j.aspen.2024.102298
CYP345D2(wrongly called CYP6K1)Tribolium castaneumlower resistance to CO2 stressaffects carbohydrate metabolism Wang et al., 2024doi.org/10.3390/insects15070502
CYP346A1,A2Tribolium castaneumno effect on phosphine toxicity Wang et al., 2020doi.org/10.1016/j.pestbp.2020.104622
CYP346B1, B2, B3Tribolium castaneumphosphine Wang et al., 2020doi.org/10.1016/j.pestbp.2020.104622
CYP347W1Phaedon cochleariae (leaf beetle) depletion in isoxazolin-5-one glucoside ester and increase in isoxazolin-5-one glucoside in the larval hemolymph (3-nitropropionic acid biosynthesis) Fu et al., 2021doi.org/10.1111/1744-7917.12944
CYP384A1Tetranychus cinnabariusfenpropathrin Shi et al., 2016doi.org/10.1111/imb.12251
CYP402B2 (wrongly called CYP6K1)Bemisia tabaci (MEAM1)abamectin Zhou et al., 2024doi.org/10.3390/insects15060399
CYP402C1Bemisia tabaciimidacloprid Guo et al.,2023doi.org/10.1111/1744-7917.13081
CYP408A1Nilaparvata lugens ethofenprox, nitenpyram,imidacloprid Yang et al., 2024doi.org/10.1016/j.pestbp.2024.105939
CYP408A3Sogatella furciferachlorpyrifos Ruan et al., 2021doi.org/10.3390/biology10080795
CYP408B1Locusta migratoriadeltamethrin Guo et al., 2012doi.org/10.1016/j.chemosphere.2011.12.061
CYP409A1Locusta migratoriadeltamethrin Guo et al., 2012doi.org/10.1016/j.chemosphere.2011.12.061
CYP3107A10 (wrongly called CYP3A24)Neoseiulus barkerichlorpyriphos (decreased toxicity) Yu et al., 2024doi.org/10.1016/j.jhazmat.2024.135163
CYP3115A1Nilaparvata lugensno effect on chlorpyrifos tox Zhang et al., 2023doi.org/10.1021/acs.jafc.2c08957
CYP3356A1 (HGT)Bradysia odoriphagaimidacloprid, thiamethoxam, β-cypermethrin Chen et al., 2019doi.org/10.1002/ps.5208
CYP3653A1Frankliniella occidentalis decreased larval survivalHan & Rotenberg, 2024 doi.org/10.1111/1744-7917.13478
CYP3828A1 (HGT)Bradysia odoriphagaclothianidin Zhang et al.,2024 doi.org/10.1021/acs.jafc.2c01315
CYP3828A1 (HGT)Bradysia odoriphagaimidacloprid, phoxim Wang et al.,2022doi.org/10.1021/acs.jafc.4c00358
CYP4174B1 (wrongly called CYP6A14X1)Dastarcus helophoroides (Coleoptera)λ-cyhalothrin Zhang et al., 2023doi.org/10.1002/ps.7319
CYP4 clan
CYP4C52v1Culex quinquefasciatuspermethrin Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP4C61Nilaparvata lugens inhibits ability to feed on YHY51 (BPH-resistant) rice Peng et al., 2017doi.org/10.3389/fphys.2017.00972
CYP4C61Nilaparvata lugens decreased weight gain on diets with tricin, hesperetin,proquamezine or TN1 rice Zhang et al., 2024doi.org/10.1016/j.jare.2024.11.006
CYP4C62Nilaparvata lugensdecreases tox of chlorpyrifos Zhang et al., 2023doi.org/10.1021/acs.jafc.2c08957
CYP4C64Bemisia tabacithiamethoxam Yang et al., 2021doi.org/10.1126/sciadv.abe5903
CYP4C64Bemisia tabaciafidopyropen Ma et al.2024doi.org/10.1016/j.jia.2024.07.027
CYP4C67Diaphorina citriimidacloprid Killiny et al., 2014doi.org/10.1371/journal.pone.0110536
CYP4C68Diaphorina citriimidacloprid Killiny et al., 2014doi.org/10.1371/journal.pone.0110536
CYP4C76Nilaparvata lugens decreased weight gain on diet with proquamezineZhang et al., 2024doi.org/10.1016/j.jare.2024.11.006
CYP4C78Nilaparvata lugens decreased weight gain on diets with tricin, hesperetin,proquamezine or TN1 rice Zhang et al., 2024doi.org/10.1016/j.jare.2024.11.006
CYP4D21 (wrongly called SXE1)Drosophila melanogaster decreased male courting and mating successFujii et al., 2008doi.org/10.1534/genetics.108.089177
CYP4D42v1Culex quinquefasciatuspermethrin Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP4E3Drosophila melanogasterMT-RNAi(but not fat body RNAi): permethrinincreased ER oxidative stress in the MTTerhzaz et al., 2015doi.org/10.1016/j.ibmb.2015.06.002
CYP4G1Drosophila melanogaster CHC biosynthesis inhibited, increased susceptibility to desiccationQiu et al., 2012doi.org/10.1073/pnas.1208650109
CYP4G1Drosophila melanogasterDDT Gellatly et al., 2015doi.org/10.1016/j.pestbp.2015.01.001
CYP4G1Drosophila melanogasterDDT Kim et al., 2018doi.org/10.1016/j.pestbp.2018.03.003
CYP4G19 Blattella germanica Chinese pyrethroid Jia Chong Qing Guo et al., 2010doi.org/10.1155/2010/517534
CYP4G19 Blattella germanica beta-cypermethrin Gao et al., 2023doi.org/10.1016/j.pestbp.2023.105703
CYP4G62Locusta migratoriamalathion, chlorpyriphos, deltamethrin, carbarylincreased susceptibility to desiccation, decreased CHC levelsWu et al., 2020doi.org/10.1002/ps.5914
CYP4G68Bemisia tabaciimidacloprid,thiamethoxam Liang et al., 2022doi.org/10.3390/agriculture12040473
CYP4G74Spodoptera frugiperdaspinetoram,fipronil,thiamethoxam,λ-cyhalothrin,emamectin benzoate Lu et al., 2024doi.org/10.1002/ps.8054
CYP4G100Bactrocera dorsalis decrease in CHC levels, accumulation of triglycerides, increased water loss, higher desiccation susceptibility Jin et al., 2022doi.org/10.1111/imb.12803
CYP4G102Locusta migratoriamalathion, chlorpyriphos, deltamethrin, carbarylincreased susceptibility to desiccation, decreased CHC levelsWu et al., 2020doi.org/10.1002/ps.5914
CYP4G70Diaphorina citriimidacloprid Killiny et al., 2014doi.org/10.1371/journal.pone.0110536
CYP4G79Harmonia axyridis lower CHC levels,effects on melanin spots Zhang et al., 2021DOI.org/10.1127/entomologia/2020/0970
CYP4L12 (wrongly called CYP4L4)Spodoptera litura decreased response to sex pheromone Feng et al., 2017doi.org/10.1111/imb.12307
CYP4P1Drosophila melanogasterDDT Seong et al.,2019doi.org/10.1016/j.pestbp.2019.06.008
CYP4P2Drosophila melanogasterDDT Seong et al.,2019doi.org/10.1016/j.pestbp.2019.06.008
CYP4Q3Leptinotarsa decemlineataimidacloprid Kaplanoglu et al., 2017doi.org/10.1038/s41598-017-01961-4
CYP4Q85 (wrongly called CYP4Q)Dastarcus helophoroides (Coleoptera)λ-cyhalothrin Zhang et al., 2023doi.org/10.1002/ps.7319
CYP4S35 (wrongly called CYP4S4)Lymantria disparemamectin benzoate Xu et al., 2024doi.org/10.1016/j.pestbp.2023.105765
CYP4AA1Solenopsis invicta flonicamid Zhang et al., 2023 doi.org/10.1016/j.pestbp.2023.105651
CYP4BN6Tribolium castaneumartemisia essential oil Gao et al., 2020
CYP4BN6Tribolium castaneumdichlorvos, (marginal effect on carbofuran) Xiong et al., 2020doi.org/10.1002/ps.5384
CYP4BW9 (wrongly called CYP4C1)Solenopsis invicta flonicamid Zhang et al., 2023 doi.org/10.1016/j.pestbp.2023.105651
CYP4CE1Nilaparvata lugensimidacloprid Zhang et al., 2016doi.org/10.1016/j.ibmb.2016.10.009
CYP4CE1Nilaparvata lugenschlorpyrifos Lu et al., 2021doi.org/10.1016/j.pestbp.2021.104800
CYP4CE1Nilaparvata lugenschlorpyrifos Zhang et al., 2023doi.org/10.1021/acs.jafc.2c08957
CYP4CE1Nilaparvata lugensnitenpyram, imidacloprid Zhang et al., 2024doi.org/10.1021/acs.jafc.3c02495
CYP4CE1Nilaparvata lugensnitenpyram, imidacloprid Zhang et al., 2024doi.org/10.1016/j.jare.2024.11.006
CYP4CJ1Aphis gossypiispirotetramat Peng et al.,2022doi.org/10.1002/ps.6818
CYP4CJ6Sitobion miscanthiimidacloprid, thiamethoxam Hu et al, 2022 doi.org/10.1017/S0007485322000037
CYP4CK1Aphis gossypiithiamethoxam, imidacloprid Lv et al., 2022doi.org/10.1021/acs.jafc.2c04867
CYP4CK1Aphis gossypiicyantraniliprole Ding et al., 2023doi.org/10.1016/j.ijbiomac.2023.126824
CYP4CL2Panonychus citripyridaben Pan et al., 2023doi.org/10.1021/acs.jafc.3c06921
CYP4CS5Bemisia tabacithiamethoxam, clothianidin Hu et al.,2024
CYP4DB1Diaphorina citriimidacloprid Killiny et al., 2014doi.org/10.1371/journal.pone.0110536
CYP4DE1Nilaparvata lugenschlorpyrifos and imidacloprid mix Xu et al., 2020
CYP4DE1Laodelphax striatellusethiprole Elzaki et al., 2015
CYP4EM1Rhodnius prolixusdeltamethrin lower survival rate also in absence of insecticidePaim et al., 2021doi.org/10.1111/imb.12737
CYP4EM10Triatoma infestans no effect on deltamethrin toxicity Dulbecco et al., 2018doi.org/10.1038/s41598-018-28475-x
CYP4EP4Varroa destructortoxicity of coumaphos DECREASED Vlogiannitis et al. 2021 doi.org/10.1073/pnas.2020380118
CYP4FB2Nilaparvata lugenschlorpyrifos Zhang et al., 2023doi.org/10.1021/acs.jafc.2c08957
CYP4FD2Sogatella furciferasulfoxaflor Wang et al., 2019doi.org/10.3390/ijms20184573
CYP4NQ26 wrongly called CYP4BN4v7Callosobruchus maculatus decrease in terminal oocyte lengthChen et al., 2024 doi.org/10.1038/s41598-024-79866-2
CYP4PR1Triatoma infestansdeltamethrin Dulbecco et al., 2021doi.org/10.1016/j.pestbp.2021.104781
CYP4ABT1 (wrongly called CYP4C1)Dastarcus helophoroides (Coleoptera)λ-cyhalothrin Zhang et al., 2023doi.org/10.1002/ps.7319
CYP313A1Drosophila melanogasterno effect on DDT toxicity Seong et al.,2019doi.org/10.1016/j.pestbp.2019.06.008
CYP325G4Culex pipiens pallens deltamethrin Xu et al. 2024doi.org/10.1021/acs.jafc.4c05708
CYP325BB1Culex pipiens pallensdeltamethrin Li et al., 2021doi.org/10.1186/s13071-021-05033-5
CYP325BC1Culex quinquefasciatusmalathion Huang et al., 2023
CYP325BG1Culex pipiensdeltamethrin Hong et al., 2014doi.org/10.1016/j.ibmb.2014.10.007
CYP325BG3Culex pipiens pallensdeltamethrin Guo et al., 2017doi.org/10.1016/j.ibmb.2017.03.006
CYP325Y6Culex quinquefasciatuspermethrin Yang et al., 2021doi.org/10.1038/s41598-021-88121-x
CYP340G2Spodoptera litura indoxacarb Li et al., 2023doi.org/10.1016/j.jhazmat.2023.132605
CYP340L16Spodoptera frugiperdatetraniliprole,spinetoram,emamectin benzoate Wang et al., 2024doi.org/10.1017/S000748532300038X
CYP340W1Plutella xylostellaabamectin Gao et al., 2016doi.org/10.3390/ijms17030274
CYP340AA4Spodoptera frugiperdaspinetoram Wang et al., 2024doi.org/10.1017/S000748532300038X
CYP340AD3Spodoptera frugiperdaspinetoram,thiamethoxam,λ-cyhalothrin,emamectin benzoate,chlorfenapyr Lu et al., 2024doi.org/10.1002/ps.8054
CYP340AX8v2Spodoptera frugiperdatetraniliprole,spinetoram Wang et al., 2024doi.org/10.1017/S000748532300038X
CYP340AX8Spodoptera lituracyantraniliprole Li et al., 2023doi.org/10.1021/acs.jafc.3c04865
CYP341B15v2Spodoptera frugiperdaspinetoram,emamectin benzoate Wang et al., 2024doi.org/10.1017/S000748532300038X
CYP341B17v2Spodoptera frugiperdatetraniliprole Wang et al., 2024doi.org/10.1017/S000748532300038X
CYP350D1Leptinotarsa decemlineatachlorantraniliprole Dumas et al., 2019doi.org/10.1002/arch.21642
CYP380C6Aphis gossypiispirotetramat Pan et al., 2018
CYP380C7Rhopalosiphum padiλ-cyhalothrin Wang et al., 2022doi.org/10.1016/j.pestbp.2022.105088
CYP380C10Nilaparvata lugens low survival,loss of cuticular hydrocarbons, no effect of RNAi for 17 other CYP4 clan P450sWang et al., 2022doi.org/10.1016/j.jinsphys.2022.104380
CYP389A1Tetranychus cinnabarinuscyflumetofen Feng et al., 2023doi.org/10.1111/1744-7917.13151
CYP389B1Tetranychus cinnabariusfenpropathrin Shi et al., 2016doi.org/10.1111/imb.12251
CYP389C2Tetranychus cinnabarinuscyflumetofen Feng et al., 2023doi.org/10.1111/1744-7917.13151
CYP389C10Tetranychus urticaeabamectin Xu et al., 2021doi.org/10.1002/ps.6130
CYP389C16Tetranychus cinnabariuscyflumetofen, pyridaben, AB-1 (active de-esterified metabolite of cyflumetofen) Feng et al., 2019doi.org/10.1002/ps.5564
CYP391A1Tetranychus cinnabariusfenpropathrin Shi et al., 2016doi.org/10.1111/imb.12251
CYP427A1Nilaparvata lugensno effect on chlorpyrifos tox Zhang et al., 2023doi.org/10.1021/acs.jafc.2c08957
CYP439A1Nilaparvata lugenschlorpyrifos and imidacloprid mix Xu et al., 2020
CYP439A2Nilaparvata lugensetofenprox Zhang et al., 2024doi.org/10.1016/j.jare.2024.11.006
CYP3093A11Triatoma infestans no effect on deltamethrin toxicity Dulbecco et al., 2018doi.org/10.1038/s41598-018-28475-x
Mito clan
CYP12D1Drosophila melanogasterDDT Gellatly et al., 2015doi.org/10.1016/j.pestbp.2015.01.001
CYP12D1Drosophila melanogasterDDT Kim et al., 2018doi.org/10.1016/j.pestbp.2018.03.003
CYP301A1Drosophila melanogaster abdominal cuticle defects at adult emergenceSztal et al., 2012doi.org/10.1371/journal.pone.0036544
CYP301A1Apis ceranathiamethoxam, dichlorvos, paraquat, deltamethrin Zhang et al., 2019doi.org/10.3389/fgene.2019.01000
CYP301B1Nilaparvata lugensb-asarone Xu et al. 2021doi.org/10.1016/j.ijbiomac.2020.12.217
CYP301B1Nilaparvata lugenspymetrozine Sun et al., 2024 doi.org/10.1016/j.pestbp.2024.106199
CYP302A1Portunus trituberculatus (Decapoda) marginal effect on 20E titer only day 2 p.i.Xie et al., 2016doi.org/10.1016/j.cbpa.2016.06.001
CYP302A1Macrobrachium nipponense (Decapoda) some decrease in E titer, some delayed molting and ovarian maturation Zheng et al., 2023doi.org/10.1016/j.jsbmb.2023.106336
CYP302A1Sogatella furcifera lower survivorship and development affected Wan et al., 2014 doi.org/10.1371/journal.pone.0086675
CYP302A1Laodelphax striatellus lower survivorship and development affected Wan et al., 2014 doi.org/10.1371/journal.pone.0086675
CYP302A1Locusta migratoria little molting failure L3 to L4 Zhang et al., 2022doi.org/10.1111/1744-7917.12907
CYP302A1Schistocerca gregaria NO effect on the development and shape of growing oocytes in adult females, or on the shape (length/width ratio) of the deposited eggs. Oviposition and hatching success were NOT negatively affected Schellens et al., 2022doi.org/10.3390/ijms23169232
CYP302A1Nilaparvata lugens no eggs hatchingZhou et al., 2020doi.org/10.1016/j.ibmb.2020.103428
CYP302A1Nilaparvata lugensgene wrongly called CYP320A1 or CYP3230A1 but is LOC111060963, 302A1 low survival on riceRout et al., 2023doi.org/10.3390/cimb45080429
CYP302A1Diaphorina citri reduced 20E titer, lower survivorship Zhang et al., 2023doi.org/10.1016/j.pestbp.2023.105361
CYP302A1Daphnia sinensis molting delay,embryonic development impairedQi et al.,2023
CYP302A1Spodoptera frugiperda larval mortality. reduced larval weight and longer developmental time when fed riceHafeez et al.2023doi.org/10.3389/fpls.2022.1079442
CYP302A1 Lasioderma serricorne (beetle) lower ecdysteroid titer, impaired development Yan et al., 2023[ 10.1127/entomologia/2023/2033
CYP302A1Calliptamus italicus (Acridid) delays egg diapause terminationZhao et al., 2024doi.org/10.1002/ps.8308
CYP302A1Solenopsis invictano effect of flonicamid (in queens)Zhang et al., 2024doi.org/10.1021/acs.jafc.4c08903
CYP314A1Schistocerca gregaria blocks 20E production,increasing E/20E ratio in hemolymph, no effect on molting Marchal et al. 2012doi.org/10.1016/j.jinsphys.2012.03.013
CYP314A1Schistocerca gregaria effect on the development and shape of growing oocytes in adult females, and on the shape (length/width ratio) of the deposited eggs. Oviposition and hatching success were negatively affected Schellens et al., 2022doi.org/10.3390/ijms23169232
CYP314A1Anopheles gambiae reduced ecdysteroid production by ovariesPondeville et al., 2013doi.org/10.1371/journal.pone.0079861
CYP314A1Leptinotarsa decemlineata larval lethality,lower 20E titer Kong et al., 2014doi.org/10.1111/imb.12115
CYP314A1Nilaparvata lugens lower 20E titer,larval mortality, ovarian growth arrestZhou et al., 2020doi.org/10.1016/j.ibmb.2020.103428
CYP314A1Locusta migratoria little molting failure L3 to L4 Zhang et al., 2022doi.org/10.1111/1744-7917.12907
CYP314A1Diaphorina citrithiamethoxam, cypermethrinreduced 20E titer, lower survivorship Zhang et al., 2023doi.org/10.1016/j.pestbp.2023.105361
CYP314A1 Culex pipiens pallensdeltamethrin Sun et al.,2019 doi:.org/10.1017/S0031182018001002
CYP314A1Tetranychus cinnabarinus lower ecdysteroid titer,lower Vg expression, reduced fecundityShen et al.,2022 doi.org/10.1111/1744-7917.12970
CYP314A1Grapholita molesta (Tortricidae)emamectin benzoate Liu et al., 2023 doi.org/10.3390/ijms242015435
CYP314A1Lasioderma serricorne (beetle) lower ecdysteroid titer, impaired development Yan et al., 2023[ 10.1127/entomologia/2023/2033
CYP314A1Bactrocera minax larval mortality, pupation failure, reduced 20E titerZhou et al., 2022doi.org/10.1002/ps.6966
CYP315A1Tetranychus cinnabarinus lower ecdysteroid titer,lower Vg expression, reduced fecundityShen et al.,2022 doi.org/10.1111/1744-7917.12970
CYP315A1Laeodelphax striatellus nymphal lethality, delayed development Wan et al., 2014doi.org/10.1002/ps.3780
CYP315A1Plutella xylostella lower 20E titer,lower Vg levelsPeng et al., 2019doi.org/10.3389/fphys.2019.01120
CYP315A1Bemisia tabaci MEAM1 lower survival of nymphs Luan et al., 2013doi.org/10.1016/j.ibmb.2013.05.012
CYP315A1Nilaparvata lugens late larval mortalityZhou et al., 2020doi.org/10.1016/j.ibmb.2020.103428
CYP315A1Portunus trituberculatus (Decapoda) some effect on 20E titer only day 4 p.i.Xie et al., 2016doi.org/10.1016/j.cbpa.2016.06.001
CYP315A1Laodelphax striatellus reduced survival, delayed developmentWan et al., 2014doi.org/10.1002/ps.3780
CYP315A1Bombyx mori pupae treated, upregulation of kynurenine biosynthesis genes but no effect egg diapause Zhu et al., 2019doi.org/10.1016/j.gene.2019.03.054
CYP315A1Locusta migratoria little molting failure L3 to L4 Zhang et al., 2022doi.org/10.1111/1744-7917.12907
CYP315A1Schistocerca gregaria effect on the development and shape of growing oocytes in adult females, and on the shape (length/width ratio) of the deposited eggs. Oviposition and hatching success were negatively affected Schellens et al., 2022doi.org/10.3390/ijms23169232
CYP315A1Diaphorina citrithiamethoxam, cypermethrinreduced 20E titer, lower survivorship Zhang et al., 2023doi.org/10.1016/j.pestbp.2023.105361
CYP315A1Lasioderma serricorne (beetle) lower ecdysteroid titer, impaired development Yan et al., 2023[ 10.1127/entomologia/2023/2033
CYP333A36Glyphodes pyloalistolfenpyrad Pan et al., 2023 PBP
CYP339A1Spodoptera litura indoxacarb Li et al., 2023doi.org/10.1016/j.jhazmat.2023.132605
CYP353D1Nilaparvata lugenschlorpyrifos and imidacloprid mix Xu et al., 2020
CYP419A1Laodelphax striatellustriflumezopyrim Wang et al., 2023doi.org/10.1016/j.pestbp.2023.105413
unclear CYP id:
comp30167, 38558, 40700 and 44013 called CYP9b2 CYP49a1 CYP12b1Bradysia odoriphagaimidacloprid Chen et al., 2018doi.org/10.1038/s41598-018-20981-2
DN2722 (6?)Megalurothrips usitatusacetamiprid Chen et al., 2023doi.org/10.3389/fphys.2023.1130389
CCG018948 wrongly called CYP6A8Aedes albopictusdeltamethrin Xu et al., 2018doi.org/10.1371/journal.pntd.0006828
CYP6A14-1 ???= Cluster–666.21614 (transcript)Sitobion avenaeimidacloprid Zhang et al., 2020doi.org/10.1016/j.cropro.2019.105014
CYP9E2-like ????Leptinotarsa decemlineataimidacloprid Naqquash et al., 2020
EEF01131148Leptinotarsa decemlineataimidacloprid Naqquash et al., 2020
CYP6UN1 ???Aphis gossypiidinotefuran Chen et al., 2020doi.org/10.1016/j.pestbp.2020.104601
CYP6BJa/b ???Leptinotarsa decemlineataimidacloprid, potato leaf extract Kalsi et al., 2017doi.org/10.1016/j.ibmb.2017.02.002
cyp3 clan, 4 genesSpodoptera litura Cheng et al., 2017doi.org/10.1038/s41559-017-0314-4
CYP6B2?Cydia pomonelladeltamethrin, azinphos methyl, NOT imidacloprid Wan et al., 2019doi.org/10.1038/s41467-019-12175-9
effects_of_p450_knockdown_by_rnai.txt · Last modified: 2025/01/12 14:11 by renefeyereisen